increased skeletal muscle glycogen level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than the normal concentration of a readily converted carbohydrate reserve in skeletal muscle (Mammalian Phenotype Ontology, MP_0010401)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010401
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Genes

9 gene mutations causing the increased skeletal muscle glycogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACACB acetyl-CoA carboxylase beta
CKM creatine kinase, muscle
CTHRC1 collagen triple helix repeat containing 1
GAA glucosidase, alpha; acid
GBE1 glucan (1,4-alpha-), branching enzyme 1
H6PD hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)
NHLRC1 NHL repeat containing E3 ubiquitin protein ligase 1
PFKM phosphofructokinase, muscle
PHKA1 phosphorylase kinase, alpha 1 (muscle)